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PDBsum entry 5i3r

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protein ligands Protein-protein interface(s) links
Transferase/transferase inhibitor PDB id
5i3r

 

 

 

 

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Contents
Protein chains
302 a.a.
Ligands
IDK ×2
PO4 ×2
Waters ×192
PDB id:
5i3r
Name: Transferase/transferase inhibitor
Title: Crystal structure of bmp-2-inducible kinase in complex with an indazole inhibitor
Structure: Bmp-2-inducible protein kinase. Chain: a, b. Synonym: bike. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: bmp2k, bike, hrihfb2017. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
2.40Å     R-factor:   0.188     R-free:   0.231
Authors: R.M.Counago,F.J.Sorrell,T.Krojer,P.Savitsky,J.M.Elkins,A.Axtman, D.Drewry,C.Wells,C.Zhang,W.Zuercher,T.M.Willson,C.H.Arrowsmith, A.M.Edwards,C.Bountra,P.Arruda,O.Gileadi,Structural Genomics Consortium (Sgc)
Key ref: R.M.Counago et al. Crystal structure of bmp-2-Inducible kinase in comple an indazole inhibitor. To be published, .
Date:
10-Feb-16     Release date:   09-Mar-16    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q9NSY1  (BMP2K_HUMAN) -  BMP-2-inducible protein kinase from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1161 a.a.
302 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.2.7.11.1  - non-specific serine/threonine protein kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction:
1. L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H+
2. L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H+
L-seryl-[protein]
+ ATP
= O-phospho-L-seryl-[protein]
+ ADP
+ H(+)
L-threonyl-[protein]
+ ATP
= O-phospho-L-threonyl-[protein]
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

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